Job Information
Medtronic Sensor Engineering Manager in Northridge, California
Careers That Change Lives
Join us in Engineering the Extraordinary as an Engineering Manager in the Sensor and Infusion Engineering R&D division at Medtronic Diabetes.
As a lead in the team, you will help in supporting the evaluation of technology and assess the feasibility of innovative sensor designs. As the team leader, you will be instrumental in providing essential project management and leadership to enable product development success.
Your role will encompass collaboration with technical program managers to provide engineering leadership. You will participate in the ideation, design, development, clinical testing, and regulatory submissions of micro-fabricated electrochemical glucose and bio-sensors. These sensors are crucial components of our next-generation diabetes management products. Your leadership will be key in validating designs and contributing towards the Medtronic mission.
In this role, you will be responsible for identifying and implementing top-tier processes and technologies, as well as fostering a culture of continuous improvement. Your leadership will focus on coaching, developing, and mentoring your team to enhance performance metrics, thereby supporting the organization’s short and long-term goals. You will also directly manage significant operational projects, ensuring that our program management and clinical practices are of the highest standard, thereby providing a competitive advantage for our business.
This is an in-person full-time position and may require travel less than 10% of the time.
The Diabetes Operating Unit focuses on improving the lives of those within the global diabetes community. As a business, we strive to empower people with diabetes to live life on their terms by delivering innovation that truly matters and providing support in the ways they need it. We’re committed to meeting people with diabetes where they are in their journey, always with an aim to make their lives easier. Our portfolio of innovative solutions is designed to provide customers greater freedom and better health, helping them achieve better glucose control, while spending less time managing their disease.
A career at Medtronic is like no other. We’re purposeful. We’re committed. And we’re driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide.
A Day in the Life
As the leader of the Clinical Oversight team, you will be accountable to the Sensor R&D leadership for overall study execution. Your responsibilities may include, but are not limited to, the following:
Oversee the design and execution of all CGM R&D pre-clinical and human feasibility studies in collaboration with clinical partners ensuring they align with the organization’s financial and competitive goals.
Maintain the study plan and schedule, engaging cross-functionally for successful completion, ensuring stakeholder engagement.
Engage, maintain, and cultivate relationships with our clinical partners both internal and external to Medtronic.
Develop mechanisms for monitoring study progress and intervening when necessary.
Provide a communication link between the clinical team, regulatory function, and the rest of the Sensor R&D organization.
Foster a deep understanding of clinical sensor signals and their integration into diabetes management systems.
Develop a robust understanding of system interdependencies as they relate to sensor signals, and drive requirements accordingly.
Maintain system and platform-level visibility to ensure seamless integration of continuous monitoring devices into standalone and closed-loop systems.
Develop clear and attainable project objectives, build project requirements, and manage the triple constraints of time, cost, and technical scope
Develop and maintain a detailed project plan for workstreams and engage with the technical team to deliver on milestones
Work across engineering teams (chemistry design, sensor electrode design, sensor manufacturing, algorithms, system engineering, clinical feasibility, etc.) to manage technical effort and design integration
Manage technical risks and issues by working with the technical team to develop and maintain risk burndown plans, tracking metrics that relate to the sensor performance goals, investigating issues and implementing solutions in a timely manner
Promote team professional development to enhance engagement, growth, job satisfaction, and organizational health.
Mentor junior staff to develop best practices to ensure process adherence and effective project management, utilizing best practice skills, as well as framing and resolving issues.
Respond to business environment demands through resource planning, resource allocation, skill set competencies, and long-term capacity planning.
Manage and track the clinical budget.
Develop communication mechanisms including storyboards and leverage PowerPoint slides to inform Senior level leadership and program stakeholders of program strategy, status, risks, next steps, etc.
Provide feedback to functional department heads during the Annual Operating Plan (AOP), strategic planning process, and the performance management process.
Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.
Bachelors Degree in Engineering or other science related field and 5+ years R&D, product development, or program/project engineering experience.
OR
Advanced Degree in Engineering or other science related field and 3+ years R&D, product development, or program/project engineering experience.
Nice to Have
BS or Advanced degree in electrochemistry, biochemistry, or material science and engineering.
Experience in medical device clinical trials in-human.
Experience connecting clinical study design to labeling impacts for products.
Understanding of clinical safety requirements and regulatory requirements for in-human studies.
Experience with regulatory submissions and FDA regulations (e.g., 510k, PMA).
Medical device product development experience, including design and manufacturing of medical devices.
Strong track record of supporting and/or leading projects.
Strong critical thinking and problem-solving skills in a team environment, coupled with the ability to interpret technical reports and statistical analysis.
Strong analytical, planning, organization, and time management skills to effectively develop and execute comprehensive programs and budgets.
Program Management Qualification: PMP Certification.
Relevant experience in product development including product concept generation, conducting trade-off analyses, requirements flowdown, subsystem integration, technical risk management, requirements verification, and clinical validation.
Experience working collaboratively at all levels in a matrix environment to build and maintain the positive relationships required to accomplish organizational goals.
Excellent written and verbal communication skills; ability to present information to cross-functional audiences including management, and write technical documents related to engineering work.
Business acumen: ability to think and act from an overall “best for the business” perspective. Results-oriented: strong sense of urgency
About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Learn more about our benefits here (http://benefits.medtronic.com/) .
This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 here .
The provided base salary range is used nationally in the United States (except in Puerto Rico and certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.
Min Salary
136000
Max Salary
204000
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.